CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Current Advancements in Anti-Cancer Chimeric Antigen Receptor T Cell Immunotherapy and How Nanotechnology May Change the Game.
Current Advancements in Anti-Cancer Chimeric Antigen Receptor T Cell Immunotherapy and How Nanotechnology May Change the Game.
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嵌合抗原受体(CAR)T 细胞免疫疗法是癌症治疗领域的前沿进展。这种创新疗法在靶向并清除恶性肿瘤方面显示出巨大潜力,尤其是白血病和淋巴瘤。
然而,尽管取得突破性成功,CAR-T 细胞疗法仍面临诸多挑战,在实体瘤治疗中尤为突出,包括如何选择合适的肿瘤抗原、管理治疗相关毒性、克服 T 细胞耗竭,以及应对高昂的治疗费用。纳米医学是纳米技术与医学交叉形成的领域,可为解决这些局限提供新策略。纳米医学已在癌症治疗中取得显著进展,包括提高药物靶向特异性、改进癌症诊断和成像技术,以及制定长期癌症预防策略。将纳米医学与 CAR-T 细胞疗法整合,有望改善 CAR-T 工程化过程中的基因递送、降低全身毒性,并减轻肿瘤微环境中的免疫抑制作用。本综述探讨 CAR-T 细胞免疫疗法单独应用的发展历程,以及纳米医学未来如何增强其疗效。
此外,综述还讨论了限制 CAR-T 细胞疗法脱靶效应和全身毒性的策略,有望改善患者耐受性和治疗结局。
Chimeric antigen receptor (CAR)-T cell immunotherapy represents a cutting-edge advancement in the landscape of cancer treatment. This innovative therapy has shown exceptional promise in targeting and eradicating malignant tumors, specifically leukemias and lymphomas.
However, despite its groundbreaking successes, (CAR)-T cell therapy is not without its challenges. These challenges, particularly pronounced in the treatment of solid tumors, include but are not limited to, the selection of appropriate tumor antigens, managing therapy-related toxicity, overcoming T-cell exhaustion, and addressing the substantial financial costs associated with treatment. Nanomedicine, an interdisciplinary field that merges nanotechnology with medical science, offers novel strategies that could potentially address these limitations.
Its application in cancer treatment has already led to significant advancements, including improved specificity in drug targeting, advancements in cancer diagnostics, enhanced imaging techniques, and strategies for long-term cancer prevention.
The integration of nanomedicine with (CAR)-T cell therapy could revolutionize the treatment landscape by enhancing the delivery of genes in (CAR)-T cell engineering, reducing systemic toxicity, and alleviating the immunosuppressive effects within the tumor microenvironment. This review aims to explore how far (CAR)-T cell immunotherapy has come alone, and how nanomedicine could strengthen it into the future.
Additionally, the review will examine strategies to limit the off-target effects and systemic toxicity associated with (CAR)-T cell therapy, potentially enhancing patient tolerance and treatment outcomes.
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